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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 739 records · Page 41
All sourcesNASA NTRSDOE OSTI
DOE OSTI2016

Radio frequency abnormal dielectric response of manganese chromite (MnCr{sub 2}O{sub 4}) nanoparticles synthesized by coprecipitation method

Highlights: • Uniform MnCr{sub 2}O{sub 4} nanoparticles synthesized by surfactant-free coprecipitation route. • XRD analysis confirmed the single spinel phase formation in the material. • Dielectric loss was found abnormal over certain lower frequencies. • AC conductivity proved the involvement of small polarons in conduction process. - Abstract: Radio frequency dielectric behavior of nanocrystalline MnCr{sub 2}O{sub 4} synthesized via surfactant-free controlled coprecipitation route has been studied. Keeping in view the necessity of particle size uniformity and phase purity for genuine performance, experimental conditions were optimized accordingly. The scanning electron micrographs of the synthesized product revealed the formation of monodispersed particle system. X-ray diffraction analysis confirmed monophasic spinel structure formation with 65 nm crystallite size. Two characteristic peaks observed between 700 cm{sup −1} and 400 cm{sup −1} in the FTIR spectrum also supported the spinel phase purity of compound. The dielectric constant was found normal, but loss tangent of the sample showed abnormal behavior with frequency. The observed dielectric behavior of the synthesized product has been explained on the basis of space-charge polarization according to Maxwell–Wagner’s model and mutual contribution of n-type &p-type charge carriers (Rezlescu model). The ac conductivity linearly increased with frequency highlighting the existence of polaron hopping.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Novel preparation of an ancient ceramic pigment BaCuSi4O10 and its performance investigation

Highlights: • The BaCuSi{sub 4}O{sub 10} (Chinese blue) was prepared firstly by coprecipitation and hydrothermal process at 180 °C for 20 h, and then sintered at 800 °C, resulting in pigment with superior performance. • The as-prepared pigment possesses bright blue coloration, preferable flower-like mesoporous microspheres morphology and qualified purity. • This novel process could fabricate the BaCuSi{sub 4}O{sub 10} pigment with broadband optical absorption and better emission in the near-infrared region. • This novel process decreases the calcination temperature compared with the traditional solid state method and also lowers the hydrothermal temperature and time compared with only a sole hydrothermal process. - Abstract: The BaCuSi{sub 4}O{sub 10} (Chinese blue) was prepared by coprecipitation and hydrothermal process at 180 °C for 20 h prior to sintering at 800 °C with a final pigment of superior performance. The crystalline configuration and microstructure of the product were characterized by XRD, FTIR, SEM and TEM. The electronic structure and the valence situation were determined by XPS. The coloration was studied with colorimeter. The absorption and the luminescence properties were examined with an UV−VIS-NIR spectrometer and a spectrofluorimeter, respectively. The results show that the BaCuSi{sub 4}O{sub 10} pigment prepared by this combined fabrication process possesses flower-like mesoporous microspheres morphology, better crystallization, clear coloration and rather qualified purity. The as-prepared BaCuSi{sub 4}O{sub 10} pigment also shows well optical property with broadband absorption and better emission in the 800–1200 nm range. Compared with traditional solid state fabrication or only sole hydrothermal process, this novel process can also reduce hydrothermal temperature and time, and decrease calcination temperature.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Blue photons excited highly chromatic red light emitting K3La(PO4)2:Pr3+ phosphors for white light emitting diodes

Highlights: • K{sub 3}La(PO{sub 4}){sub 2}:Pr{sup 3+} phosphors were investigated as an alternative for red light. • Highly chromatic red emission was realized upon blue excitation. • The phosphor has high color purity ∼ 97.8% and yield ∼27%. - Abstract: Highly chromatic blue photons excited red emitting K{sub 3}La(PO{sub 4}){sub 2}:Pr{sup 3+} (0–1.8 mol%) phosphors were synthesized by solution combustion method. The resulted phosphors showed peanut like morphology and had a monoclinic phase with space group P2{sub 1}/m. The photoluminescence studies disclosed that the phosphor emits red light due to the {sup 1}D{sub 2} → {sup 3}H{sub 4} and {sup 1}D{sub 2} → {sup 3}H{sub 5} transition of the Pr{sup 3+} ions under blue photons excitation. The optimal concentration for the Pr{sup 3+} ions were optimized to be 1.2 mol% after which concentration quenching occurred. Dipole-dipole interaction among the dopant ions was found to be responsible for the concentration quenching. X-ray photoelectron spectroscopy results depicted that Pr was present in the (+3) valance state in the phosphor. The photometric results suggest that the phosphor with a high color purity ∼ 97.8% and enough quantum yield ∼27% could be an eventual choice as the red component for white light emitting diodes.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Chemical bath deposition of single crystal SnS nanobelts on glass substrates

Highlights: • Single crystal SnS nanobelts were deposited by CBD method. • The morphologies of SnS nanobelts were regulated by mole ratios of precursors and pH levels. • The photo-electrical properties of SnS nanobelts were characterized. - Abstract: SnS nanobelt thin films were deposited on glass substrates in acidic solution by chemical bath deposition (CBD) method. The belt-like morphologies of as-deposited SnS thin films were characterized by scanning electron microscope (SEM) and transmission electron microscopy (TEM). X-ray diffraction (XRD) and Raman measurements were carried out to confirm the crystal structures and phase purities of SnS nanobelt thin films. The morphologies and phase purities of SnS thin films were influenced greatly by the tin and sulfur precursors. The bandgaps of SnS nanobelts were determined to be 1.39–1.41 eV by UV–vis absorption and photoluminescence (PL) spectra. Current-voltage ((IV)) and current-time ((I-T)) characteristics were studied to demonstrate the photoelectric performances of SnS nanobelt thin films.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Structural, morphological, optical and magnetic properties of Ag3(2+x)InxNb4-xO11+δ (0.25 ≤ x ≤ 1.0) nanoparticles synthesized by sol–gel method

Highlights: • Novel Ag{sub 3 (2+x)} In{sub x}Nb{sub 4-x}O{sub 11+δ} nanoparticles were synthesized by sol-gel method and studied their optical magnetic properties. • XRD studies confirm the single-phase monoclinic lattice structure with P2/m space group. • Morphology, purity and homogeneity of samples were confirmed by SEM images, EDX and X-ray mapping. • The absorption spectra and tauc plots confirms the semiconductor nature of the samples. • Magnetic studies reveals the ferromagnetic behavior of the samples at room temperature. - Abstract: Herein, we report the structure, morphology, optical and magnetic properties of novel Ag{sub 3 (2+x)} In{sub x}Nb{sub 4-x}O{sub 11+δ} (0.25 ≤ × ≤ 1.0; A1–A4) nanoparticles prepared by sol-gel technique. The samples were studied using X-ray diffraction, electron microscopy, diffuse reflectance spectroscopy, vibrating sample magnetometer, and electron spin resonance. X-ray diffraction studies confirm the formation of monoclinic lattice type with P2/m space group. Purity and homogeneity of the samples were confirmed by X-ray mapping. The semiconductor nature of the samples was identified by optical absorption spectra which indicate an inter-band transition from the oxygen 2p to niobium 4d electronic states. The magnetization plots reveal the room temperature ferromagnetic behavior of the samples.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Flux growth and magneto-transport properties of cubic antiperovskite Ca3PbO single crystals

Highlights: • Antiperovskite Ca{sub 3}PbO is predicted to be a three-dimensional Dirac fermion system. • Cubic crystals, 1 mm in size, were obtained by a Ca-self-flux method. • The crucible and sealing method were critical factors to reduce carrier density. • Shubnikov-de Haas oscillations were clearly observed, indicating its high purity. - Abstract: We report the single crystal growth of cubic antiperovskite Ca{sub 3}PbO by a Ca-self-flux method. Cubic crystals, 1 mm in size, were successfully obtained through the use of iron crucibles sealed in stainless steel capsules. The crucible material and sealing method were found to be critical factors for achieving large crystals with low carrier density. The crystals were subsequently characterized by powder and single-crystal x-ray diffraction experiments, electron-probe microanalysis, and Hall effect measurements. Through the use of short stainless steel rods as tight caps for the crucible and fillers to occupy extra space in the capsule, the Ca evaporation loss of the flux, which contributes to Ca vacancy formation, was effectively reduced. Hence, the hole carrier density in the single crystal was reduced to 4.0 × 10{sup 19} cm{sup −3}. The crystal synthesized under optimized growth conditions showed clear Shubnikov-de Haas oscillations, indicating its high purity and homogeneity.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2022

Two-stage membrane-based process utilizing highly CO 2 -selective membranes for cost and energy efficient carbon capture from coal flue gas: A process simulation study

Membrane technology for CO 2 capture has become an attractive strategy due to its cost and energy efficiency and low materials costs. In the past decade, membrane-based process designs for post-combustion power plant CO 2 capture have been developed, utilizing existing highly CO 2 -permeable membranes with relatively low CO 2 /N 2 selectivity (<50), and have obtained reasonably economic carbon capture. However, few membrane-based process designs were proposed for moderate to highly CO 2 -selective membranes (CO 2 /N 2 selectivity of 50–300, and >300, respectively), which have vastly emerged in recent years, such as various facilitated transport membranes (FTMs). Herein, we proposed a two-stage membrane-base process design targeting economic carbon capture from coal-fired flue gas. This process design features the utilization of highly CO 2 -selective membranes for one-stage CO 2 enrichment to 95% dry-base purity in the first stage and recycle of the remaining CO 2 by a highly CO 2 -permeable membrane in the second stage, in order to achieve economic CO 2 capture with 90% capture rate and >95% CO 2 product purity. Through an integration-iteration membrane model and the Aspen Plus process simulation, a sensitivity study of operating pressures (feed and permeate pressures) and membrane properties (CO 2 permeance and CO 2 /N 2 selectivity) was conducted. Critical CO 2 /N 2 selectivity of 300–400 was found for the highly CO 2 -selctive membranes to meet the demand for cost and energy efficient results. The lowest possible membrane area of 4.8 × 10 5 m 2 and fractional energy of 19.3% were obtained, which is comparable to or even more attractive than reported membrane-based process designs. Here, this work provides a new membrane process design option for highly CO 2 -selective membranes and gives insights on the influence of membrane performance and operation condition.

42 ENGINEERING↗
DOE OSTI2025

Selective concentration of multivalent cations via electrodialysis through tandem membranes

Selective electrodialysis is attractive for recovering and recycling valuable ions. However, most studies in this field focus on membranes that are selective for monovalent ions. Multivalent cations preferentially partition into cation-exchange membranes, but low mobilities and concentration polarization limit electrodialysis selectivities for these cations. This work employs electrodialysis through an “in-series” combination of a Nafion membrane and a multilayer polyelectrolyte film (MPF)-coated Nafion membrane to concentrate and isolate La 3+ or Mg 2+ from monovalent ions. The bare Nafion membrane gives a La 3+ /Na + selectivity up to 4 (depending on conditions), which enables concentration of La 3+ with a high current efficiency. The MPF-coated membrane allows selective passage of Na + while rejecting La 3+ to increase the purity of the concentrated multivalent cation. For example, the concentration of La 3+ in the accumulation solution can reach 9 times its original concentration in the feed solution with a purity of 93 mol% (99 wt%) when starting with equimolar mixtures of NaNO 3 and La(NO 3 ) 3 . This study examines how the separation varies with the type of polyelectrolyte, the applied voltage, and the composition of feed, accumulation, and cathode solutions. Here, a high nitric acid concentration (0.5 M) in the cathode compartment allows monovalent anions to pass through the MPF-coated Nafion membrane to maintain the electroneutrality of the accumulation solution. With a low acid concentration (0.04 M) in the cathode chamber, water splitting occurs at the MPF-coated membrane and La(OH) 3 precipitates.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2022

Crystallization of potassium-zeolites in organic-free media

A ubiquitous phenomenon in zeolite synthesis is the generation of polymorphs leading to either single or multi-phase products. The use of organic structure-directing agents (OSDAs) often ensures a high degree of phase purity for a desired zeolite; however, OSDAs can be economically and environmentally prohibitive. The use of alkali metals as inorganic structure-directing agents (ISDAs) is a common alternative, although reductions in polymorph specificity and/or purity in organic-free media are significant limitations. Developing more controlled, facile synthesis strategies without the aid of OSDAs relies on understanding how zeolite growth conditions impact polymorph selection and alter the physicochemical properties of crystalline products. Relatively few studies of organic-free syntheses have systematically explored potassium growth media. Here, in this study, we examine synthesis conditions that promote the formation of five K-zeolites: CHA, LTL, MER, EDI, and BPH frameworks. Time-resolved analyses reveal distinct trends in crystallization kinetics and interzeolite transformations for potassium compared to prior studies that have largely focused on Na-zeolites. We also highlight methods to achieve nanosized crystals and markedly reduce crystallization times for zeolites, such as chabazite, which are notoriously difficult to synthesize in organic-free media at reasonable timescales. Collectively, these findings identify routes to control K-zeolite polymorphism and provide general design strategies to tailor their crystallization.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Recommended Nuclear Data for the Production of Selected Therapeutic Radionuclides

Increasing interest in the treatment of human disease by means of targeted radionuclide-based therapies requires an accurate understanding of achievable yields and quantification of realisable degrees of purity. Important studies within a more extensive Coordinated Research Project of the International Atomic Energy Agency (IAEA CRP) have included in-depth assessments and evaluations of all available measured cross-section data for ten nuclear reactions leading to the formation of 131 Cs, 131 Ba, 225 Ac, 225 Ra, 227 Th, 227 Ac, 230 U and 230 Pa for various on-going and proposed therapeutic applications in nuclear medicine. Equivalent studies were also undertaken of possible reactions to produce the 178W /low-spin 178m Ta generator system that has been clinically applied in diagnosis by means of SPECT - these particular cross-section studies and recommendations are included in this paper for completeness. All available measured data have been critically reviewed and assessed to produce statistically consistent datasets. Selected datasets have been fitted by a least-squares method with Padé approximations of variable order to evaluate the production cross sections and corresponding uncertainties. New measurements have been made in some instances, and reported data have been adjusted to accommodate new nuclear decay or monitor reaction data which altered the original reported quantities adversely. Insufficient measured data are available in many cases to permit a reliable evaluation of cross sections, and these instances are discussed. Finally, recommended therapeutic radionuclide production reaction data and their uncertainties are available on the Web page of the IAEA Nuclear Data Section at www-nds.iaea.org/radionuclides/ and also at the IAEA medical portal www-nds.iaea.org/medportal/.

63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTAN↗
DOE OSTI2019

Improved Cumulative Fission Yield Measurements with Fission Spectrum Neutrons on 235 U

Two isotopically-characterized targets of high-purity (99.84±0.03%) 235 U-oxide and a neutron dosimetry package were exposed to a pulsed neutron irradiation using the Godiva critical assembly at the National Criticality Experiments Research Center. Following irradiation, the fissioned targets were counted with a broad-energy germanium detector. Estimates of the total fissions for each target were made using measurements of well-known fission products. The total fission values were then used to measure the fission yields of 21 fission products with half-lives between 636 and 119,700 seconds. Mean values of seventeen of the measured fission products fell within the 95% confidence level of the Evaluated Nuclear Data Files VII.1/b (ENDF/B-VII.1) using the larger of the two uncertainties: 84g Br, 89 Rb, 91 Sr, 93 Y, 97 Zr, 101 Mo, 105 Ru, 128 Sn, 129 Sb, 130g Sb, 131 Sb, 131m Te, 133 I, 135 I, 141 Ba, 142 Ba, and 142 La. Seven isotopes were measured to better precision than is listed in the ENDF/B-VII.1 database: 89 Rb, 93 Y, 128 Sn, 129 Sb, 130g Sb, 131m Te, and 133 I. Four of the measured isotopes were found to be statistically different from the ENDF/B-VII.1 database: 94 Y, 134 Te, 134 I, and 138 Xe. Two of the isotopic analyses conducted in this paper fit the parent and daughter data simultaneously. The parent-daughter pairs measured in this way were the 134 Te/I and 142 Ba/La pairs. The fission yield results obtained in this way are unique, especially for 134 I, because the parent and daughter half-lives are so close. Here, given the limited number of direct measurements of the 134 Te/I pair from fast neutron induced fission and the seemingly high estimate for 134 Te from previous work, it is likely that the value in this paper is more accurate; however, additional measurements of this pair are needed to validate this assertion.

42 ENGINEERING↗
DOE OSTI2016

Validation of gamma-ray detection techniques for safeguards monitoring at natural uranium conversion facilities

Recent IAEA circulars and policy papers have sought to implement safeguards when any purified aqueous uranium solution or uranium oxides suitable for isotopic enrichment or fuel fabrication exists. Under the revised policy, IAEA Policy Paper 18, the starting point for nuclear material under safeguards was reinterpreted, suggesting that purified uranium compounds should be subject to safeguards procedures no later than the first point in the conversion process. In response to this technical need, a combination of simulation models and experimental measurements were employed to develop and validate concepts of nondestructive assay monitoring systems in a natural uranium conversion plant (NUCP). In particular, uranyl nitrate (UO 2 (NO 3 ) 2 ) solution exiting solvent extraction was identified as a key measurement point (KMP), where gamma-ray spectroscopy was selected as the process monitoring tool. The Uranyl Nitrate Calibration Loop Equipment (UNCLE) facility at Oak Ridge National Laboratory was employed to simulate the full-scale operating conditions of a purified uranium-bearing aqueous stream exiting the solvent extraction process in an NUCP. Nondestructive assay techniques using gamma-ray spectroscopy were evaluated to determine their viability as a technical means for drawing safeguards conclusions at NUCPs, and if the IAEA detection requirements of 1 significant quantity (SQ) can be met in a timely way. This work investigated gamma-ray signatures of uranyl nitrate circulating in the UNCLE facility and evaluated various gamma-ray detector sensitivities to uranyl nitrate. These detector validation activities include assessing detector responses to the uranyl nitrate gamma-ray signatures for spectrometers based on sodium iodide, lanthanum bromide, and high-purity germanium detectors. The results of measurements under static and dynamic operating conditions at concentrations ranging from 10–90 g U/L of natural uranyl nitrate are presented. A range of gamma-ray lines is examined, including attenuation for transmission measurement of density and concentration. It was determined that transmission-corrected gamma-ray spectra provide a reliable way to monitor the 235 U concentration of uranyl nitrate solution in transfer pipes in NUCPs. Furthermore, existing predictive and analysis methods are adequate to design and realize practical designs. The 137 Cs transmission source employed in this work is viable but not optimal for 235 U densitometry determination. Validated simulations assessed the viability of 133 Ba and 57Co as alternative densitometry sources. All three gamma-ray detectors are viable for monitoring natural uranium feed; although high-purity germanium is easiest to interpret, it is, however, the least attractive as an installation instrument. Overall, for monitoring throughput in a facility such as UNCLE, emulating the uranium concentration and pump speeds of the Springfields conversion facility in the United Kingdom, an uncertainty of less than 0.17% is required in order to detect the diversion of 1 SQ of uranyl nitrate through changes in uranium concentration over an accountancy period of one year with a detection probability of 50%. As a result, calibrated gamma-ray detection systems are capable of determining the concentration of uranium content in NUCPs, it is only in combination with verifiable operator declarations and supporting data, such as flow rate and enrichment, that safeguards conclusions can be drawn.

98 NUCLEAR DISARMAMENT, SAFEGUARDS, AND PHYSICAL P↗
DOE OSTI2016

High voltage testing for the Majorana Demonstrator

The Majorana Collaboration is constructing theMajorana Demonstrator, an ultra-low background, 44-kg modular high-purity Ge (HPGe) detector array to search for neutrinoless double-beta decay in 76Ge. The phenomenon of surface micro-discharge induced by high-voltage has been studied in the context of theMajorana Demonstrator. This effect can damage the front-end electronics or mimic detector signals. To ensure the correct performance, every high-voltage cable and feedthrough must be capable of supplying HPGe detector operating voltages as high as 5 kV without exhibiting discharge. R&D measurements were carried out to understand the testing system and determine the optimum design configuration of the high-voltage path, including different improvements of the cable layout and feedthrough flange model selection. Every cable and feedthrough to be used at the Majorana Demonstrator was characterized and the micro-discharge effects during theMajorana Demonstrator commissioning phase were studied. A stable configuration has been achieved, and the cables and connectors can supply HPGe detector operating voltages without exhibiting discharge.

high-voltage↗
DOE OSTI2018

FRAM v5.2 estimation of plutonium and uranium isotopics using digitized 3-D position-sensitive CdZnTe detectors

Gamma-ray spectroscopy is an important tool used in international safeguards to measure plutonium and uranium isotopics. Recently developed, digital, 3-D position-sensitive CdZnTe gamma-ray spectrometers are promising for safeguards, offering improved performance over commonly available CdZnTe systems, with energy resolutions approaching that of high-purity germanium. CdZnTe gamma-ray spectra from plutonium and uranium samples were processed using the commercially available software FRAM v5.2, a tool that estimates plutonium and uranium isotopics from high-purity germanium spectra, across a wide range of materials. Furthermore using digital CdZnTe systems 239 Pu/ 240 Pu isotopic composition and effective 240 Pu percentage are evaluated to within less than 3 sigma statistical measurement uncertainty across reactor to weapons-grade samples, while low and highly-enriched uranium are easily distinguished.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2018

Investigation of Compton scattering for gamma beam intensity measurements and perspectives at ELI-NP

Compton γ-ray sources have been used for over 30 years with new facilities being under construction or proposed. The gamma beam system under implementation at the Extreme Light Infrastructure - Nuclear Physics facility in Romania will deliver brilliant γ-ray beams with energies up to 19.5 MeV. Several instruments for measuring the parameters of the γ-ray beam are under development at ELI-NP. One of these instruments based on a High Purity Germanium detector is typically used for beam energy measurements at other facilities. Here we investigate the use of a High Purity Germanium detector to continuously monitor the intensity of the ELI-NP gamma beam by measuring the inelastic scattering of photons. This technique relies on both experimental and simulated data and it has been successfully tested during a recent experiment at the High Intensity γ-ray Source facility.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2019

GEANT4 models of HPGe detectors for radioassay

Radiation transport models of two high purity germanium detectors, GeII and GeIII, located at the University of Alabama have been created in GEANT4 (Agostinelli et al., 2003) [1].These detectors have been used extensively for radioassay measurements of materials used in various low background experiments. The two models have been validated against actual data under several scenarios typically seen in radioassay measurements. Furthermore, the systematic uncertainties of the models for GeII and GeIII are estimated to be ~12% and ~9% respectively.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2022

Status of the SABRE South experiment at the Stawell underground physics laboratory

The SABRE (Sodium iodide with Active Background REjection) experiments aim to detect an annual rate modulation from dark matter interactions in ultra-high purity NaI(Tl) crystals. The SABRE South experiment is located at the Stawell Underground Physics Laboratory (SUPL), Australia, and is the first deep underground laboratory in the Southern Hemisphere. SABRE South is designed to disentangle seasonal or site-related effects from the dark matter-like modulated signal first observed by DAMA/LIBRA in the Northern Hemisphere using an active veto and muon detection system. It is a partner to the SABRE North effort at the Laboratori Nazionali del Gran Sasso (LNGS). SABRE South is instrumented with ultra-high purity NaI(Tl) crystals immersed in a linear alkyl benzene (LAB) based liquid scintillator veto, further surrounded by passive steel and polyethylene shielding and a plastic scintillator muon veto. Significant work has been undertaken to understand the experimental backgrounds and performance of the crystals. The SABRE South experiment is under construction, and will be commissioned from late 2022 to early 2023. We will present the final design of SABRE South, the status of its construction, its expected background, and its sensitivity to a DAMA/LIBRA like modulation. We will also present recent quenching factor measurements of sodium nuclear recoils in NaI(Tl) crystals measured at the Heavy Ion Accelerator Facility, and a report on the status of SUPL.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2021

Particle-in-cell techniques for the study of space charge effects in the Advanced Cryogenic Gas Stopper

The Facility for Rare Isotope Beams, FRIB, will significantly increase the rates and varieties of rare isotopes compared to those presently available at existing rare-isotope facilities. The production of stopped beams via the current generation of linear gas stopping devices available is not well matched to the beam intensities that will be available at FRIB. Many experiments that make use of reaccelerated beams, from the ReA facility, greatly benefit from having the highest-intensity, rare-isotope beams possible. Some experiments would also benefit greatly from stopped beams with improved purity. In this paper, the intensity bottlenecks of FRIB’s newest linear gas stopper are studied via experiment and simulation in support of a future detailed conceptual design of a next-generation linear gas stopper that can provide rare-isotope beams with rates of 10^8 pps, a factor of 50 higher than the current state-of-the-art system, with improved beam purity.

43 PARTICLE ACCELERATORS↗